VOLU-SOL ORANGE G-6(GILLS-MOD
K-Number: K822038 · 1982-08-03
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Device Summary
Frequently Asked Questions
What is the VOLU-SOL ORANGE G-6(GILLS-MOD?
VOLU-SOL ORANGE G-6(GILLS-MOD is a medical device that received FDA 510(k) clearance on 1982-08-03. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K822038.
When did VOLU-SOL ORANGE G-6(GILLS-MOD receive FDA 510(k) clearance?
VOLU-SOL ORANGE G-6(GILLS-MOD received FDA 510(k) clearance on 1982-08-03, under 510(k) number K822038.
Who is the listed applicant for VOLU-SOL ORANGE G-6(GILLS-MOD?
The FDA 510(k) record lists Volu Sol Medical Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOLU-SOL ORANGE G-6(GILLS-MOD?
The FDA product code for VOLU-SOL ORANGE G-6(GILLS-MOD is HZH.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Volu Sol Medical Industries as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HZH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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